Clinical Trials Logo

Clinical Trial Summary

This study will investigate the effect of a 6-week stretching intervention, consisting of a combination of a 2-week casting period and a home-based stretching program of the plantar flexors and hamstrings, on muscle and tendon lengths, range of motion, stiffness, and functional muscle strength. The study will include patients with spastic cerebral palsy aged between 4 and 11 years old with a Gross Motor Function Classification Score (GMFCS) level between I and III.


Clinical Trial Description

This study will investigate the effect of a 6-week stretching intervention on muscle and tendon lengths, range of motion, stiffness, and functional muscle strength. The program consists of a 2-week casting period of the lower legs and a home-based stretching program of the hamstrings, followed by a 4-week stretching program of both the plantar flexors and hamstrings. The aim is twofold: (1) determine whether a 6-week stretching program for the plantar flexors and knee flexors leads to changes in the morphological muscle and tendon properties of the medial gastrocnemius and semitendinosus, ankle and knee range of motion, muscle strength, gait and gross motor function; and (2) determine the correlation between baseline morphological muscle and tendon properties and the changes in the primary outcome parameters (ankle range of motion and stiffness). The program will start with a 2-week period of stretching casts for the ankle plantar flexors, combined with a passive stretch program for the hamstrings, followed by a passive and active stretch program for both muscle groups for the remaining 4 weeks. The durations and frequencies for passive and active stretching are based on guidelines published by our own research group and on programs applied by previous research. The program will be set-up as a supervised home-based program on top of the usual care. The morphological muscle and tendon parameters, strength, spasticity, stiffness as well as gross motor function will be assessed before and after the entire 6-week stretching program. At the time of cast removal (after 2 weeks), only the morphological muscle and tendon parameters will be evaluated. This study includes an intervention and control group which will be group-matched based on diagnosis, GMFCS level and age. The study will include patients with spastic cerebral palsy between 4 and 11 years old and a GMFCS level between I and III. Thirty children with a clinical indication for casting of the lower limb will be included in the intervention group and 30 children without an indication for a specific intervention will be included in the control group. Children in the control group will continue their usual care or normal routine treatment, i.e. physiotherapy and orthotic devices. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04904094
Study type Interventional
Source Universitaire Ziekenhuizen KU Leuven
Contact Britta Hanssen, dr.
Phone +3216341016
Email britta.hanssen@kuleuven.be
Status Recruiting
Phase N/A
Start date February 1, 2020
Completion date February 1, 2026

See also
  Status Clinical Trial Phase
Recruiting NCT05571033 - Operant Conditioning of the Soleus Stretch Reflex in Adults With Cerebral Palsy N/A
Completed NCT00011024 - Prospective Studies of the Use of Self Hypnosis, Acupuncture and Osteopathic Manipulation on Muscle Tension in Children With Spastic Cerebral Palsy Phase 2
Recruiting NCT05810779 - Dynamic Surface Exercise and Trunk Targeted Training in Children With Spastic Cerebral Palsy N/A
Completed NCT01049581 - Effects of Pediatric Aquatic Therapy in Children With Spastic Cerebral Palsy N/A
Completed NCT04634136 - Full-spectrum Medical Cannabis for Treatment of Spasticity in Patients With Severe Forms of Cerebral Palsy N/A
Recruiting NCT06070233 - Radiosurgery Treatment for Spasticity Associated With Stroke, SCI & Cerebral Palsy N/A
Completed NCT01815814 - Therapeutic Potential of Myofascial Structural Integration in Children With Cerebral Palsy N/A
Recruiting NCT05113433 - Effects of Different Time Period of Standing Frame on Spasticity and Gait in Children With Spastic Cerebral Palsy. N/A
Recruiting NCT03676439 - Lateral Cord Magnetic Stimulation For Refractory Spastic Cerebral Palsy Phase 2/Phase 3
Completed NCT03708757 - Effect of Post Isometric Relaxation Technique & Eccentric Muscle Contraction on Hamstring Spasticity in CP N/A
Not yet recruiting NCT03529682 - Circuit Training in Children With Cerebral Palsy N/A
Not yet recruiting NCT06407856 - Dual Task Training in Spastic Cerebral Palsy N/A
Not yet recruiting NCT06407869 - Effects of Functional Progressive Strength Training in Children With Spastic Cerebral Palsy N/A
Not yet recruiting NCT06407921 - Whole Body Vibration and BOSU Ball in Spastic Cerebral Palsy N/A
Completed NCT04078321 - Evaluation of Multifocal Transcutaneous Electrical Stimulation for Self-treatment Among Children With Cerebral Palsy N/A
Active, not recruiting NCT06330311 - Effectiveness of Whole-Body Vibration N/A
Terminated NCT00955877 - Extended-release Epidural Morphine for Acute Post-operative Analgesia Following Selective Dorsal Rhizotomy in Children N/A
Completed NCT02359799 - Robotic Rehabilitation of Cerebral Palsy N/A
Not yet recruiting NCT05340439 - INcobotulinumtoxina in ChIldren Upper and Lower Limb sPasticITy (INCIPIT) Phase 2
Completed NCT01147653 - A Randomized Study of Autologous Umbilical Cord Blood Reinfusion in Children With Cerebral Palsy Phase 2